A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735322



Internal ID20511264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36515097..36515403hg38UCSC Ensembl
chr7:36554703..36555009hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277224
Samples
Known GenesAOAH
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735322
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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